TNFに関する我々の知識と再学習すべきこと
1Lund Stem Cell Center, Lund University, Lund, Sweden; Division of Molecular Medicine and Gene Therapy, Institution for Laboratory Medicine, Lund University, Lund, Sweden.
Stem cell reports
|February 27, 2026
まとめ
腫瘍壊死因子(TNF)は骨髄を抑制する可能性があるが、造血幹細胞(HSC)への影響は複雑である。TNFは、長期的な再生能力を損なうことなく、HSCを一時的に再プログラムすることができる。
科学分野:
- 免疫学
- 血液学
- 細胞生物学
背景:
- 腫瘍壊死因子(TNF)は、伝統的に造血に有害であると見なされてきた。
- 以前の研究では、TNFが骨髄および造血幹細胞(HSC)を抑制すると示唆されていた。
研究 の 目的:
- TNFの造血における役割を再評価すること。
- TNFのHSCおよび前駆細胞への微妙な影響を調査すること。
主な方法:
- TNFの細胞型、文脈、および時間依存的な効果を検討した。
- 前駆細胞の刈り込みとHSCの再プログラムに焦点を当てて分析した。
主要な成果:
- TNFの造血への影響は一様には否定的ではない。
- TNFは前駆細胞を選択的に刈り込むことができる。
- TNFはHSCを一時的に再プログラムし、長期的な再生能力を維持することができる。
結論:
- TNFの造血における役割は複雑で文脈依存的である。
- TNFは、純粋に抑制的であるというよりも、幹細胞機能において調節的な役割を果たしている可能性がある。
さらに関連する動画
関連する概念動画
NF-κB-dependent Signaling Pathway
10.1K
The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The...
NF-κB-dependent Signaling Mechanism
The...
10.1K
Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF
660
Tumor Necrosis Factor (TNF), a proinflammatory cytokine, contributes significantly to the inflammation seen in Crohn's disease. It exists as soluble TNF and membrane-bound TNF, with actions mediated through TNF receptors (TNFR). TNFR activation leads to the release of proinflammatory cytokines, T-cell activation, collagen production, and leukocyte migration, all contributing to inflammation in Crohn's disease. Anti-TNF monoclonal antibodies, namely infliximab (Remicade), adalimumab...
660
Cytotoxic T Cells-mediated Immune Response
7.7K
Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
7.7K
T Cell Types and Functions
2.9K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
2.9K
TGF - β Signaling Pathway
10.7K
The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors...
10.7K
T Cell Activation and Clonal Selection
16.7K
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
Naive T cells that have not yet encountered an antigen express two primary CD...
16.7K


